Thiol-Ene Click Synthesis of Adsorption Functionalized Poly(Ionic Liquid)s: Influence of the Mole Fraction of Pendant Enes

Adsorption functionalized poly(ionic liquid)s could be thiol-ene click synthesized within surfactant-free ionic liquid microemulsions. However, the influence of the mole fraction of pendant enes on the as-prepared polymer is still unclear. Herein, the influence of the mole fraction of pendant enes on the molecular structure, surface morphology, thermostability and adsorption performance of poly(ionic liquid)s were investigated in detail. To characterize the as-prepared polymers, FTIR, NMR, TGA, DSC, SEM and UV–vis were used, and the adsorption isotherm/kinetics studies were carried out. The results show that the mole fraction of pendant enes had a significant difference on the characterization of poly(ionic liquid)s. The lower mole fraction of pendant enes donated lower T10% value, slower degradation rates and lower Tg, and the value of 0.30 was the boundary of forming structure with various beading sizes and structure with various irregularly shaped apertures. In addition, poly(ionic liquid)s with different mole fraction of pendant enes all showed excellent adsorption performance to DR, also indicate remarkable potential in the application of dying wastewater treatment.

An efficient click synthesis of chalcones derivatized with two 1-(2-quinolon-4-yl)-1,2,3-triazoles

Chalcones derivatized with 1-(2-quinolonyl)-1,2,3-triazoles were synthesized by reaction of 4-azido-2-quinolones with 1-phenyl-3-(4-propargyloxyphenyl)prop-2-en-1-one, or by aldol reaction of 4-{[1-(2-oxo-1,2-dihydroquinolin-4-yl)-1H-1,2,3-triazol-4-yl]methoxy}benzaldehydes with acetophenone. Whereas, chalcones bearing two 1-(2-quinolonyl)-1,2,3-triazoles were synthesized by reaction of 1,3-bis(4-propargyloxyphenyl)prop-2-en-1-one with 4-azido-2-quinolones, or by aldol condensation between 4-{4-[(4-acetylphenoxy)methyl]-1H-1,2,3-triazol-1-yl}quinolin-2(1H)-ones and 4-{[1-(2-oxo-1,2-dihydroquinolin-4-yl)-1H-1,2,3-triazol-4-yl]methoxy}benzaldehydes.

Post-Synthetic ‘Click’ Synthesis of RAFT Polymers with Pendant Self-Immolative Triazoles

<div> <div> <div> <p>Self-immolative linkers offer efficient mechanisms for deprotecting ‘caged’ functional groups in response to specific stimuli. Herein we describe a convenient ‘click’ chemistry method for introducing pendant self-immolative linkers to a polymer backbone through post-polymerization modification. The intro duced triazole rings serve both to anchor the stimuli-cleavable trigger groups to the polymer backbone, while also forming a functional part of the self-immolation cascade. We investigate the polymerization kinetics, post-synthetic modification, and self-immolation mechanism of a model polymer system, and discuss avenues for future studies on poly-pendant self-immolative triazoles as a modular, stimuli-responsive macromolecule platform. </p> </div> </div> </div>